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Ann Oncol. 2013;24(4):1026-31.

Phase II trial of everolimus for the treatment of nonclear-cell renal cell carcinoma.

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제1저자 고영일 · 교신저자 이세훈

PMID 23180114 DOI 10.1093/annonc/mds582 IF 80.4 혈액종양내과
소속 (1)
  1. Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Abstract

BACKGROUND We investigated the efficacy of everolimus against nonclear-cell renal cell carcinoma (nccRCC). Patients and methods Patients with nccRCC received 10-mg everolimus once daily until disease progression or unacceptable toxicity.

PATIENTS who had received a VEGF- tyrosine kinase inhibitor (TKI) previously were included.

RESULTS A total of 49 patients were enrolled. Twenty-three patients (46.9%) received prior anti-VEGF agents. A partial response was observed in five patients (10.2%) and stable disease in 25 patients (51.0%). The disease progressed in 16 patients (32.7%) despite the administration of everolimus. Two of the five patients who showed an objective response to everolimus had chromophobe carcinoma, whereas two had papillary carcinoma and one had unclassifiable carcinoma. Thirty-six patients experienced disease progression during follow-up, and the median progression-free survival (PFS) was 5.2 months. Chromophobe RCC patients seemed to have longer PFS than nccRCC patients with the other histological subtypes (P = 0.084). Previous VEGF-TKI treatment did not influence the efficacy of everolimus, and the toxicity profiles were in line with previous reports.

CONCLUSION Everolimus shows certain efficacy against nccRCC, particularly in patients with chromophobe RCC, and prior treatment with a VEGF-TKI appears not influencing the outcome of everolimus therapy in nccRCC patients. ClinicalTrials.gov number NCT00830895.

그 밖의 정보
출판 형태
Clinical Trial, Phase II, Journal Article
저널
Annals of oncology : official journal of the European Society for Medical Oncology · eISSN 1569-8041
전자 출판
2012-11-23
MeSH
Adult · Aged · Antibodies, Monoclonal, Humanized / administration & dosage · Antineoplastic Agents / administration & dosage · Bevacizumab · Carcinoma, Renal Cell / drug therapy / mortality / pathology · Disease-Free Survival · Everolimus · Female · Humans · Immunosuppressive Agents / administration & dosage · Kidney Neoplasms / drug therapy / mortality / pathology · Male · Middle Aged · Protein Kinase Inhibitors / administration & dosage · Sirolimus / administration & dosage / analogs & derivatives · Treatment Outcome
Substances
Antibodies, Monoclonal, Humanized · Antineoplastic Agents · Immunosuppressive Agents · Protein Kinase Inhibitors · Bevacizumab · Everolimus · Sirolimus
데이터
ClinicalTrials.gov: NCT00830895